Label: ANTI BACTERIAL MOISTURIZING HAND SANITIZER POMEGRANATE AND BLACKBERRY- alcohol gel

  • NDC Code(s): 62670-6857-0
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 2, 2026

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  • Active Ingredient

    Alcohol 70%

  • Purpose

    Antiseptic

  • Use

    Decreases bacteria on hands.

  • Warnings

    Flammable: Keep away from flame or high heat.

  • WARNINGS

    For external use only.

  • WHEN USING

    When using this product keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Rub a dime sized drop into hands.

  • INACTIVE INGREDIENT

    Water (Aqua, Eau), Fragrance (Parfum), Dimethicone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isopropyl Myristate, Hydroxypropylcellulose, Aminomethyl Propanol, Mannitol, Cellulose, Dimethiconol, Laureth-4, Laureth-23, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Silica, Kaolin, Retinyl Palmitate, Caprylic/Capric Triglyceride, Hydroxypropyl Methylcellulose, Titanium Dioxide (CI 77891), Ultramarines (CI 77007).

  • SPL UNCLASSIFIED SECTION

    Bath & Body Works, Distr., 95 West Main Street
    New Albany, OH 43054, 1-800-395-1001
    pat. www.bbwinc.com/patents

  • PRINCIPAL DISPLAY PANEL

    MABHS Pomegranate and Blackberry

  • INGREDIENTS AND APPEARANCE
    ANTI BACTERIAL MOISTURIZING HAND SANITIZER  POMEGRANATE AND BLACKBERRY
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6857
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-6857-029 mL in 1 BOTTLE; Type 0: Not a Combination Product06/09/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/09/2025
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    MCP TN, LLC118929829manufacture(62670-6857)
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